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Clinical Trials in Turkey / NCT07634900
Recruiting Not applicable

Comparison of the Efficacy of Inferior Alveolar Nerve Block and Digital Anesthesia in Pulpectomy of Mandibular Permanent Molars in Children

NCT07634900 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-04-01
Last updated
2026-06-09

Condition(s) studied

Pulpitis - IrreversiblePulpitis - Reversible

Investigational drug(s) / intervention(s)

Computer-Controlled Digital AnesthesiaInferior Alveolar Nerve Block

Computer-Controlled Digital Anesthesia: Participants requiring emergency endodontic treatment for mandibular permanent molars will receive conventional inferior alveolar nerve block anesthesia using a conventional dental syringe and 4% articaine hydrochloride with 1:100,000 epinephrine.

Inferior Alveolar Nerve Block: Participants requiring emergency endodontic treatment for mandibular permanent molars will receive computer-controlled intraosseous digital anesthesia using the SleeperOne computer-controlled local anesthesia delivery system and 4% articaine hydrochloride with 1:100,000 epinephrine.

Study summary

This study aims to compare the effectiveness of inferior alveolar nerve block (IANB) and computer-controlled digital anesthesia in achieving adequate anesthesia in pediatric patients presenting with acute dental pain and requiring emergency endodontic treatment of mandibular permanent molars. Achieving profound anesthesia in such cases can be challenging due to acute inflammation.

Participants will be randomly assigned to receive either conventional IANB or digital anesthesia. Pain perception during the procedure will be assessed using validated pain scales. In addition, physiological parameters including heart rate and blood pressure will be recorded to evaluate the stress response associated with each anesthesia technique. Anesthesia success will be determined based on the absence of pain during treatment and the need for supplemental anesthesia.

The findings of this study are expected to provide evidence-based guidance for selecting the most effective and comfortable anesthesia technique in pediatric dental patients.

Eligibility

Sex
ALL
Min age
6 Years
Max age
14 Years
Healthy volunteers
No
Inclusion Criteria: * Children aged 6-14 years * Patients presenting with acute dental pain * Patients requiring emergency endodontic treatment in mandibular permanent molars * Cooperative patients who allowed clinical procedures * Patients whose parents/legal guardians provided informed consent Exclusion Criteria: * Patients with systemic diseases affecting pain perception * Patients with known allergy to local anesthetic agents * Patients who used analgesics within 12 hours before treatment * Patients with non-restorable teeth * Patients with a history of behavioral management problems preventing treatment

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Inonu University Faculty of Dentistry Malatya Malatya Recruiting

More Inonu University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07634900 on ClinicalTrials.gov ↗ ← All trials in Turkey